Gene Map - Chromosome: 3 - OMIM

OMIM Gene/Loci: 815 - 824 of 1,008 on Chromosome 3 (All Entries)

Location
(from NCBI, GRCh38)
Gene/Locus Gene/Locus name Gene/Locus
MIM number
Phenotype Phenotype
MIM number
Inheritance Pheno
map
key
Comments Mouse
symbol
(from MGI)
3:159,069,319
3q25.32
IQCJ IQ motif-containing protein J 611622 Iqcj
3:159,273,244
3q25.32-q25.33
SCHIP1 Schwannomin-interacting protein 1 619206 Schip1
3:159,300,001
3q25.33
PBC1 Biliary cirrhosis, primary, 1 109720 Biliary cirrhosis, primary, 1 109720 AD 2 associated with rs6441286 and rs574808
3:159,988,835
3q25.33
IL12A Interleukin-12A (natural killer cell stimulatory factor-1, cytotoxic lymphocyte maturation factor-1, p35) 161560 Il12a
3:160,256,986
3q25.33
IFT80, KIAA1374, WDR56, SRTD2, ATD2 Intraflagellar transport 80 611177 Short-rib thoracic dysplasia 2 with or without polydactyly 611263 AR 3 Ift80
3:160,399,650
3q25.33
CAPC Chromosome-associated protein C 605575 Smc4
3:160,404,588
3q25.33
MIR15B Micro RNA 15B 619572
3:160,435,503
3q25.33
TRIM59, RNF104, MRF1, IFT80L Tripartite motif-containing protein 59 616148 Trim59
3:160,495,007
3q25.33
KPNA4, QIP1 Karyopherin alpha-4 602970 Kpna4
3:160,514,907
3q25.33
SCARNA7 Small Cajal body-specific RNA 7 615644

OMIM Gene/Loci: 815 - 824 of 1,008 on Chromosome 3 (All Entries)

Location
(from NCBI, GRCh38)
Gene/Locus Gene/Locus name Gene/Locus
MIM
number
Phenotype Phenotype
MIM
number
Inheritance Pheno
map
key
Comments Mouse
symbol
(from MGI)
3:159,069,319-159,266,307
3q25.32
IQCJ IQ motif-containing protein J 611622 Iqcj
3:159,273,244-159,897,359
3q25.32-q25.33
SCHIP1 Schwannomin-interacting protein 1 619206 Schip1
3:159,300,001-161,000,000
3q25.33
PBC1 Biliary cirrhosis, primary, 1 109720 Biliary cirrhosis, primary, 1 109720 Autosomal dominant 2 associated with rs6441286 and rs574808
3:159,988,835-159,996,019
3q25.33
IL12A Interleukin-12A (natural killer cell stimulatory factor-1, cytotoxic lymphocyte maturation factor-1, p35) 161560 Il12a
3:160,256,986-160,399,225
3q25.33
IFT80, KIAA1374, WDR56, SRTD2, ATD2 Intraflagellar transport 80 611177 Short-rib thoracic dysplasia 2 with or without polydactyly 611263 Autosomal recessive 3 Ift80
3:160,399,650-160,434,953
3q25.33
CAPC Chromosome-associated protein C 605575 Smc4
3:160,404,588-160,404,685
3q25.33
MIR15B Micro RNA 15B 619572
3:160,435,503-160,449,786
3q25.33
TRIM59, RNF104, MRF1, IFT80L Tripartite motif-containing protein 59 616148 Trim59
3:160,495,007-160,565,571
3q25.33
KPNA4, QIP1 Karyopherin alpha-4 602970 Kpna4
3:160,514,907-160,515,236
3q25.33
SCARNA7 Small Cajal body-specific RNA 7 615644


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